Tag | Content |
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EnhancerAtlas ID | HS184-15131 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:6800880-6802120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr19:6801934-6801947 | CTGATTTGCATAT | + | 6.5 | POU4F2 | MA0683.1 | chr19:6801069-6801085 | ATCATCAATTATTCAC | - | 6.42 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_17561 | chr19:6798623-6803806 | CD4p_CD25-_CD45RAp_Naive | SE_18804 | chr19:6799714-6804369 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 6801016 | 6802093 | chr19 | 6801116 | 6801467 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I006799 | chr19 | 6799599 | 6804367 |
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Enhancer Sequence | GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA CCCAGCCGCT 60 CACCATCTCT TTGTCGCCTG CATGGCACCA TTCTCTCCTG TACCACCCCA AAGCCTTACC 120 AGGTGCCTCC TGCATTTAAC CAGGTCCCAT AGCTCTCTGT GCTTCCCGGC ACACCCTCTC 180 ACCACCCTCA TCATCAATTA TTCACCTTGC TGACTGCTTA GTGTTTGTCT CCTGGCTGGA 240 TTACATAAGC CCTGTAAGGG CAGAGCTCTG TTTGTCTTGA TCACCATTAG GTTCTGGTGC 300 TTGGCATACA GTAGGCATTC CACACATGCT TGCTGAATTA ATGCATGACC GGGTCTGGGG 360 TGCTGGGTTT CACACCAGGC TCTACCGCAA ACATTGGGTC AAGTATTTTC ATTCCCGACG 420 TACAGATGAG TCAATTGAAT CAACGGAAAG CAAAATGATC CCATCCAAGC TCCCTCAACT 480 TGCCGGGCTG GTCTGGGAGT CGAACCAGAT CTGCCTGACC CTCCCACCGG TGCTGAAAAG 540 TGGAGTGTGT GCTGGGGTGG TAGGGGATGG GGCAGAAGAG AGACGGGCTT CCTCACAGAA 600 GGGTTTGAGG GCTAGGATGA GGCGTGCACA CTCTGCACCC CTGCTTCGGA GCTTTGAAAG 660 GGTGCACAGC ACACCCGCCC TCTCTGGGAA CCCTCGGGAG CTTGAGGTTG CCTGATGAAG 720 GGGCTGATGG GTTGAACGCA AAGGGCCCCT CCACCCACCC TTTTTTCTAT CTCCCCAACC 780 AAGCCCTGGT AACAGGCATT TCCGGTTTCC GGCCGGCTCC CTGGTGCTGG GGTGGGGGTG 840 GGGAGTTGAT TGCTGCCGTC GTGCTTGGCT CTGGGTCCCC TTCTCCCAGA CCCCAGAGGC 900 CTCTGTCCCT GCACACTGCT TCCCCGAAGG AGCGTGGAAA GCCAGCCGAC CTTTCTGGCT 960 CTTTCTTCAT CTTGGGCAGG GGTTTTGTTG ATGGGAGGCT GGCTGGCAAA TGGGGAAGAA 1020 TGAACCTCAG GGTTCACCGC AGTGCGCCTG GGTGCTGATT TGCATATGGG CACGATGCCA 1080 GCACAGTGGG TGCCCGCCTC TTCCTGGAGG AAGGAAGAGG GGCACTGAGG GGGGTTGCCC 1140 CCAGCAGGGA GGAACCGTCC TCATAATGCC TCTCCTACGT TTGTTTAAAG GACCATCATT 1200 CTCAGCAAAC TATAGCAAGG ACAAAAAACC AAACACCGCA 1240
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